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FDA 510(k)

VOSS DISPOSABLE CORONARY BYPASS FLUSHING CANNULA

K-Number: K896338 · 1990-05-17

ApplicantVoss Medical Products
Decision Date1990-05-17
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VOSS DISPOSABLE CORONARY BYPASS FLUSHING CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Voss Medical Products. It received FDA 510(k) clearance on 1990-05-17 under 510(k) number K896338. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VOSS DISPOSABLE CORONARY BYPASS FLUSHING CANNULA?

VOSS DISPOSABLE CORONARY BYPASS FLUSHING CANNULA is a medical device that received FDA 510(k) clearance on 1990-05-17. The listed applicant is Voss Medical Products. The 510(k) number is K896338.

When did VOSS DISPOSABLE CORONARY BYPASS FLUSHING CANNULA receive FDA 510(k) clearance?

VOSS DISPOSABLE CORONARY BYPASS FLUSHING CANNULA received FDA 510(k) clearance on 1990-05-17, under 510(k) number K896338.

Who is the listed applicant for VOSS DISPOSABLE CORONARY BYPASS FLUSHING CANNULA?

The FDA 510(k) record lists Voss Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VOSS DISPOSABLE CORONARY BYPASS FLUSHING CANNULA?

The FDA product code for VOSS DISPOSABLE CORONARY BYPASS FLUSHING CANNULA is DWF.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Voss Medical Products as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K932187PRONE POSITIONERK932186BYPASS LEG POSITIONERK885161VOSS VEIN CLAMPK895369VOSS GRAFT MARKER

Related Devices (Code: DWF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260195Elongated One-Piece Arterial (EOPA) 3D™ Arterial CannulaeMedtronic, Inc.K250937Venous Return CannulaeLivaNova USA, Inc.K260043Smart Reactors Camouflage Coated Extracorporeal Cardiopulmonary Tubing Set (SR180C)Smart ReactorsK253203Retrograde Coronary Sinus Perfusion CannulaeMedtronic, Inc.K253671Dual Stage Venous CannulaeSorin Group Italia S.R.L.K253998Clearview Intracoronary ShuntsMedtronic, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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